| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:50450329-50450412 | Rare:32 | ||||
| chr7:55018862-55019140 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:55019326-55019355 | Rare:11 | ||||
| chr7:55365893-55366076 | Rare:76 | ||||
| chr7:55572448-55572635 | Common:1; Rare:67 | ||||
| chr7:56051375-56051978 | Common:1; Rare:211; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:65873267-65873552 | Common:1; Rare:88 | ||||
| chr7:66114769-66114904 | Common:1; Rare:66 | ||||
| chr7:66115221-66115397 | Rare:43 | ||||
| chr7:66682007-66682210 | Common:6; Rare:97 | ||||
| chr7:66921120-66921460 | Common:1; Rare:100 | ||||
| chr7:66996570-66996850 | Common:2; Rare:56 | ||||
| chr7:73308773-73308884 | Rare:47 | ||||
| chr7:73522253-73522488 | Common:1; Rare:71 | ||||
| chr7:73557491-73557576 | Rare:21 |